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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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LYMPHOSEP, LYMPHOCYTE SEPARATION MEDIA — 2 UDI-DI variants, IVDR

MD Atlas
BIO WEST

Data from EUDAMED, last updated May 19, 2026

LYMPHOSEP, LYMPHOCYTE SEPARATION MEDIA

3770026925L0560PQ

2 UDI-DI variants

IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]IVDR Class A

Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Manufacturer: BIO WEST

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Device characteristics

Reagent

Identity & classification

Basic UDI-DI: 3770026925L0560PQ
Device name: LYMPHOSEP, LYMPHOCYTE SEPARATION MEDIA
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Version date: May 25, 2022

Manufacturer & authorised representative

Manufacturer

Name: BIO WEST
SRN: FR-MF-000024000
Country: France
Email: biowest@biowest.net
Phone: +33(0)241464242

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01G3XNW72Q7K978VQFAF525873

Format

Summary

29 columns included

Trade name
Basic UDI-DI
UDI-DI code
Risk category
Applicable legislation
Status
Organization name
SRN
Reference / catalog number
Additional product description
Intended medical purpose
Placed on the market (country)
Market info update date
Sterile
Single use
Contains latex
Reprocessed single-use
Direct marking
CMR substance
Endocrine disruptor
Annex XVI applicable
Sterilization
OEM applicable
EMDN codes
Last updated
Basic UDI-DI device name
Basic UDI-DI device model
Basic UDI-DI implantable
Basic UDI-DI reagent

LYMPHOSEP, LYMPHOCYTE SEPARATION MEDIA - 100ML03770026925003
LYMPHOSEP, LYMPHOCYTE SEPARATION MEDIA - 500ML03770026925010